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Year | Number of Results |
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1998 | 1 |
1999 | 1 |
2024 | 0 |
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Autosomal dominant cerebellar ataxia type I: oculomotor abnormalities in families with SCA1, SCA2, and SCA3.
J Neurol. 1999 Sep;246(9):789-97. doi: 10.1007/s004150050456.
J Neurol. 1999.
PMID: 10525976
Clinical Trial.
Oculomotor phenotypes in autosomal dominant ataxias.
Buttner N, Geschwind D, Jen JC, Perlman S, Pulst SM, Baloh RW.
Buttner N, et al.
Arch Neurol. 1998 Oct;55(10):1353-7. doi: 10.1001/archneur.55.10.1353.
Arch Neurol. 1998.
PMID: 9779665
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